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Leader Acid Reducer Complete

Generic: Famotidine, Calcium Carbonate, Magnesium Hydroxide

OTC
Histamine-2 Receptor Antagonist✓ FDA-verified
View full FDA label ↗
Leader Acid Reducer Complete is a chewable tablet that helps relieve heartburn caused by acid indigestion and sour stomach. It works by reducing the amount of acid your stomach produces, which can help ease discomfort. For adults and children aged 12 and older, you should chew one tablet before swallowing, and you should not take more than two tablets in a 24-hour period. It's important not to use this medication if you have trouble swallowing food or if you experience vomiting with blood, as these could be signs of a serious condition. Additionally, if you are taking prescription medications, especially antacids, you should check with your doctor or pharmacist to avoid any interactions.
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Uses

  • heartburn associated with acid indigestion. sour stomach.
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Dosage

Adults and children 12 years and over: chew 1 tablet before swallowing.
Do not swallow tablet whole; chew completely.
Do not use more than 2 chewable tablets in 24 hours.
Children under 12 years: ask a doctor.
Always follow your doctor's specific instructions for your dose.
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Side effects

Common

Common side effects may include mild stomach discomfort

Serious

Serious side effects include trouble swallowingvomiting bloodor bloody stools
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Warnings

⚠ Important warnings

  • Do not use if allergic to famotidine or other acid reducers.
  • Do not use if you have trouble swallowing food or bloody stools.
  • Ask a doctor if you have had heartburn over 3 months.
  • Consult a doctor if experiencing chest pain or shortness of breath.
  • Ask a doctor if pregnant or breastfeeding.

Ask about this product

Answers pulled from the FDA label only.

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Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).